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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3913754copy number variation1nstd102humanLikely benign GRCh38 chr6: 144,418,941-144,464,407 , GRCh37 chr6: 144,740,077-144,785,543 , NCBI36 chr6: 144,781,770-144,827,236 UTRN
    nsv6636653copy number variation1nstd102humanUncertain significance GRCh37 chr6: 144,758,945-144,907,222 , GRCh38.p12 chr6: 144,437,809-144,586,086 UTRN
    nsv6313556copy number variation1nstd102humanUncertain significance GRCh37 chr6: 144,739,063-145,350,329 , GRCh38.p12 chr6: 144,417,927-145,029,193 UTRN
    nsv4456533copy number variation1nstd102humanUncertain significance GRCh37 chr6: 145,116,452-145,377,537 , GRCh38.p12 chr6: 144,795,316-145,056,401 UTRN
    nsv3924459copy number variation1nstd102humanUncertain significance GRCh38 chr6: 144,418,941-144,485,393 , GRCh37 chr6: 144,740,077-144,806,529 , NCBI36 chr6: 144,781,770-144,848,222 UTRN
    nsv6314278complex chromosomal rearrangement5nstd102humanLikely pathogenic GRCh37 chr2: 181,120,972-181,120,972 , GRCh37 chr2: 186,920,618-186,920,618 , GRCh37 chr2: 186,920,668-186,920,668 , GRCh37 chr2: 181,120,915-181,120,915 , GRCh37 chr6: 147,816,319-147,816,319 , GRCh37 chr6: 160,668,625-160,668,625 , GRCh37 chr6: 144,917,096-144,917,096 , GRCh37 chr6: 144,917,096-144,917,096 , GRCh37 chr6: 147,816,319-147,816,319 , GRCh37 chr6: 160,668,627-160,668,627 , GRCh38.p12 chr2: 186,055,941-186,055,941 , GRCh38.p12 chr2: 180,256,188-180,256,188 , GRCh38.p12 chr2: 186,055,891-186,055,891 , GRCh38.p12 chr2: 180,256,245-180,256,245 , GRCh38.p12 chr6: 160,247,593-160,247,593 , GRCh38.p12 chr6: 160,247,595-160,247,595 , GRCh38.p12 chr6: 147,495,183-147,495,183 , GRCh38.p12 chr6: 147,495,183-147,495,183 , GRCh38.p12 chr6: 144,595,960-144,595,960 , GRCh38.p12 chr6: 144,595,960-144,595,960 UTRN, SLC22A2, 1 more genes
    nsv6636322copy number variation1nstd102humanUncertain significance GRCh37 chr6: 144,703,479-145,689,316 , GRCh38.p12 chr6: 144,382,343-145,368,180 UTRN, SNORA98, 2 more genes
    nsv3918457copy number variation1nstd102humanUncertain significance GRCh37 chr6: 145,085,583-145,930,265 , NCBI36 chr6: 145,127,276-145,971,958 , GRCh38 chr6: 144,764,447-145,609,129 UTRN, TRQ-TTG4-1, 3 more genes
    nsv4350212copy number variation1nstd102humanPathogenic GRCh37 chr6: 135,239,633-146,997,510 , GRCh38.p12 chr6: 134,918,495-146,676,374 UTRN, LOC100131041, 146 more genes
    nsv3891146copy number variation1nstd102humanPathogenic GRCh37 chr6: 139,513,020-150,389,231 , GRCh38.p12 chr6: 139,191,883-150,068,095 UTRN, UST, 131 more genes
    nsv3916499copy number variation1nstd102humanPathogenic NCBI36 chr6: 136,359,437-146,708,473 , GRCh37.p13 chr6: 136,317,744-146,666,780 , GRCh38.p12 chr6: 135,996,606-146,345,644 UTRN, SLC35D3, 127 more genes
    nsv3890752copy number variation1nstd102humanPathogenic GRCh37 chr6: 144,075,695-152,337,005 , GRCh38.p12 chr6: 143,754,558-152,015,870 UTRN, LOC105378052, 109 more genes
    nsv3904637copy number variation1nstd102humanPathogenic GRCh37 chr6: 144,947,731-150,266,155 , GRCh38.p12 chr6: 144,626,595-149,945,019 UTRN, LOC107986660, 59 more genes
    nsv3912178copy number variation1nstd102humanPathogenic NCBI36 chr6: 142,070,748-145,748,578 , GRCh37.p13 chr6: 142,029,055-145,706,885 , GRCh38.p12 chr6: 141,707,918-145,385,749 UTRN, GJE1, 40 more genes
    nsv3877040copy number variation1nstd102humanPathogenic GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698 UTRN, LOC105378061, 2914 more genes
    nsv3879811copy number variation1nstd102humanPathogenic GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083 UTRN, RNU6-411P, 2910 more genes
    nsv3887898copy number variation2nstd102humanPathogenic GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394 UTRN, SOD1P1, 2905 more genes
    nsv3889814copy number variation1nstd102humanPathogenic GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382 UTRN, ITPR3, 2905 more genes
    nsv3911993copy number variation1nstd102humanPathogenic NCBI36 chr6: 133,900,102-166,209,023 , GRCh38 chr6: 133,537,271-165,875,545 , GRCh37 chr6: 133,858,409-166,289,033 UTRN, LOC105369171, 418 more genes
    nsv3915150copy number variation1nstd102humanPathogenic NCBI36 chr6: 124,322,082-156,156,864 , GRCh37.p13 chr6: 124,280,383-156,115,172 , GRCh38.p12 chr6: 123,959,238-155,794,038 UTRN, KATNA1, 422 more genes
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